Abstract
The oxidation of methylphenyl sulfide, benzothiophene, and dibenzothiophene with hydrogen peroxide in the presence of crown ethers was studied. The major product of the oxidation was methylphenyl sulfoxide. The reaction was retarded by the addition of amino acids, which formed 1: 1 complexes with the crown ethers. The oxidation of the diesel fraction with hydrogen peroxide can decrease the sulfur content in it.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
